FLEX-Trial: Prospective Sonographic Assessment Of Healing Process Following Suture of Profound Flexor Tendon Due to Traumatic Rupture of FDP-Tendon in Zone II.

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01013428

Enrollment

Registered

2009-11-13

Start date

2009-11-30

Completion date

2016-01-31

Last updated

2016-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tendon Injury

Keywords

Traumatic Rupture of Tendon

Brief summary

To prospectively assess the healing process following suture of profound fexor tendon due to traumatic rupture of FDP-Tendon in Zone II by ultrasound.

Interventions

OTHERUltrasound

Ultrasound will be used to evaluate tendons.

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* All patients with traumatic rupture of FDP-tendon in zone II.

Exclusion criteria

* \< 18years; * Fracture; * crush injury; (partial) amputation; * RA; * CPPD; * CP;

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026